Progress in Heterocyclic Chemistry
eBook - ePub

Progress in Heterocyclic Chemistry

  1. 702 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Progress in Heterocyclic Chemistry

Book details
Table of contents
Citations

About This Book

Progress in Heterocyclic Chemistry (PHC), Volume 29, is the latest in this annual review series commissioned by the International Society of Heterocyclic Chemistry (ISHC). Volumes in the series contain both highlights of the previous year's literature on heterocyclic chemistry and articles on new developing topics of particular interest to heterocyclic chemists.

The highlight chapters in Volume 29 are all written by leading researchers in their field and these chapters constitute a systematic survey of the important original material reported in the literature of heterocyclic chemistry in 2016. As with previous volumes in the series, Volume 29 will enable academic and industrial chemists, and advanced students, to keep abreast of developments in heterocyclic chemistry in a convenient way.

  • Recognized as the premiere review of heterocyclic chemistry
  • Includes contributions from leading researchers in the field
  • Provides a systematic survey of the important 2016 heterocyclic chemistry literature
  • Presents articles on new and developing topics of interest to heterocyclic chemists

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Yes, you can access Progress in Heterocyclic Chemistry by Gordon Gribble,John A. Joule in PDF and/or ePUB format, as well as other popular books in Physical Sciences & Organic Chemistry. We have over one million books available in our catalogue for you to explore.

Information

Publisher
Elsevier
Year
2017
ISBN
9780081023112
Topic
Physical Sciences
Subtopic
Organic Chemistry

Table of contents

  1. Cover image
  2. Title page
  3. Table of Contents
  4. Copyright
  5. Contributors
  6. Foreword
  7. Editorial Advisory Board Members Progress in Heterocyclic Chemistry
  8. Chapter 1. Recent Advances in the Synthesis of Benzimidazol-2-ones via Rearrangements
  9. Chapter 2. Use of Rhodium Carbenoid Intermediates for Dipolar Cycloaddition Chemistry
  10. Chapter 3. Three-Membered Ring Systems
  11. Chapter 4. Four-Membered Ring Systems
  12. Chapter 5.1. Five-Membered Ring Systems: Thiophenes and Se/Te Derivatives
  13. Chapter 5.2. Five-Membered Ring Systems: Pyrroles and Benzo Analogs
  14. Chapter 5.3. Five-Membered Ring Systems: Furans and Benzofurans
  15. Chapter 5.4. Five-Membered Ring Systems: With More Than One N Atom
  16. Chapter 5.5. Five-Membered Ring Systems: With N and S Atom
  17. Chapter 5.6. Five-Membered Ring Systems: With O and S (Se, Te) Atoms
  18. Chapter 5.7. Five-Membered Ring Systems With O and N Atoms
  19. Chapter 6.1. Six-Membered Ring Systems: Pyridine and Benzo Derivatives
  20. Chapter 6.2. Six-Membered Ring Systems: Diazines and Benzo Derivatives
  21. Chapter 6.3. Triazines, Tetrazines, and Fused Ring Polyaza Systems
  22. Chapter 6.4. Six-Membered Ring Systems: With O and/or S Atoms
  23. Chapter 7. Seven-Membered Rings
  24. Chapter 8. Eight-Membered and Larger Rings
  25. Index